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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameRX ACCULINK & ACCULINK CAROTID STENT SYSTEMS
Classification Namestent, carotid
Generic Namecarotid stent system and embolic protection system
ApplicantABBOTT VASCULAR-VASCULAR SOLUTIONS
PMA NumberP040012
Supplement NumberS019
Date Received07/14/2006
Decision Date09/20/2006
Product Code
NIM[ Registered Establishments with NIM ]
Advisory Committee Cardiovascular
Supplement Type135 review track for 30-day notice
Supplement Reason process change: manufacturing
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for changes to the manufacturing process for bonding the tip bump to the guidewire lumen in rx acculink and acculink carotid stents.
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